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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376767Generated: October 31, 2026

2-Iodoaniline → HCID 21753017, compound

https://huagongshe.com/reaction/1376767

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-IodoanilineHCID 11995—
Reactant4,5-Bis(trimethylsilyloxy)cyclohexa-1,4-diene-1,2-dicarboxylic acid dimethyl esterHCID 10022190—
SolventAcetic AcidHCID 176—
ProductHCID 21753017HCID 21753017—

Reaction Steps

A solution of 2.4 g (6 mmol) of 4,5-bis(trimethylsilyloxy)cyclohexa- 1,4-diene- 1,2-dicarboxylic acid dimethyl ester (Example 1a) and 5.3 g (24 mmol) of 2-iodoaniline in 24 ml of glacial acetic acid ii boiled under reflux for 2 hours. The reaction mixture is cooled, the solvent is evaporated off and the dark-brown residue is dissolved in dichloromethane and the solution is washed in succession with 20 ml of 1N HCl, 50 ml of saturated NaHCO3 and twice with 20 ml of water, dried with sodium sulfate and concentrated by evaporation. The residue obtained after concentration by evaporation is chromatographed on silica gel with ethyl acetate/hexane 2:1 and the product fractions are concentrated by evaporation, yielding the title compound in the form of a yellow foam: 1H-NMR (DMSO-d6): δ=7.91 (dxd, J1 =8, J2 =1, 2H) 7.39 (d×d×d, J1 =10, J2 =8, J3 =1, 2H), 7.32 (br s, 2H), 7.22-7.05 (m, 2H), 7.01 (s, 2H), 6.88 (t×d, Jt =8, Jd =1, 2H), 3.73 (s,6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05663336
Source datasetuspto-grants-1997_09
ORD IDord-e8144a8e40164f34a11e79a5cf5e66c3
Source noteuspto-grants-1997_09